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dbVar

Database of genomic structural variation

nsv7099287

Organism: Homo sapiens

Study:nstd231 (Ali et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:18,569

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 218 SVs from 41 studies. See in: genome view

Remapped(Score: Perfect):72,635,901-72,654,469

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099287	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	72,635,901	72,654,469
nsv7099287	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	73,210,039	73,228,607

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18792929	deletion	SNP array	SNP genotyping analysis
nssv18792931	deletion	SNP array	SNP genotyping analysis

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18792929	Remapped	Perfect	NC_000013.11:g.(72 635901_?)_(?_72654 469)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	72,635,901	72,654,469
nssv18792931	Remapped	Perfect	NC_000013.11:g.(72 635901_?)_(?_72654 469)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	72,635,901	72,654,469
nssv18792929	Submitted genomic		NC_000013.10:g.(73 210039_?)_(?_73228 607)del	GRCh37 (hg19)		NC_000013.10	Chr13	73,210,039	73,228,607
nssv18792931	Submitted genomic		NC_000013.10:g.(73 210039_?)_(?_73228 607)del	GRCh37 (hg19)		NC_000013.10	Chr13	73,210,039	73,228,607

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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